Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (C)

Chromosome 1:7963666 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs835733, rs1173412, rs659776

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 10 transcripts and has 2508 sample genotypes.

Variant displays